Mechanochemical Synthesis of Sodium-Ion Conducting Chloride NaTaCl6

Abstract

All-solid-state sodium batteries have been attracting attentions owing to their high energy density and safety. Solid electrolytes play a significant role in the electrochemical performances of all-solid-state batteries. Chloride-based solid electrolytes are particularly important for achieving high energy densities because of their high oxidation stability, ionic conductivity, and formability. Fewer sodium-ion conducting chlorides have been developed compared to lithium-ion conducting materials. It is necessary to discover the chlorides as the end-member of sodium-ion conductors. In this study, we report the development of a new NaTaCl6 chloride as an end-member sodium-ion conductor with high ionic conductivity. NaTaCl6 sample was mechanically prepared using a planetary ball mill apparatus. The X-ray diffraction patterns of the obtained sample displayed a broad pattern similar to the reported NaTaCl6 (ICSD#36519), suggesting that the sample contains both amorphous and crystalline phases. The reference intensity ratio method was used to investigate the weight ratios of the amorphous phases in the sample. The ratio was approximately 45 %. Transmission electron microscopy observations suggested that the sample consisted of the amorphous matrix and crystalline with the crystallite size of approximately 20 nm. The electrical conductivities of the pelletized samples were measured using two-terminal AC electrochemical impedance spectroscopy. The sample pellets were prepared by uniaxial pressing at 360 MPa without heat treatment. The pellet sample had the relative density of 85 % (powder density: 3.32 g cm–3, pellet density: 2.83 g cm–3). The sample shows σ 25ºC of 6.2×10–5 S cm–1, and the activation energy of 0.37 eV. To determine the NaTaCl6 onset oxidation voltage (OOV), linear sweep voltammetry measurement was carried out. The OOV of the sample at 60 ºC was 3.8 V vs. Na15Sn4. To demonstrate the high oxidation stability of NaTaCl6 in all-solid-state sodium batteries, it was used in a positive electrode by mixing Na3V2(PO4)3 as the active material and the buffer layer. The cell exhibited an initial reversible capacity of 96 mAh g–1 and stable cycling after 40 cycles with the capacity retention of 99.5 %. A 3.3 V all-solid-state sodium battery without oxide solid electrolytes was successfully operated. In this study, the NaTaCl6 electrolyte was developed with a high ionic conductivity and oxidation stability.Acknowledgement: This work was partly supported by JSPS KAKENHI (Grant Numbers: JP21H04701 and JP19H05816) and MEXT Program: Data Creation and Utilization-Type Material Research and Development Project Grant Number JPMXP1122712807.